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直接重复序列处的免疫球蛋白重链基因缺失:核苷酸序列及其对mRNA积累的影响。

An immunoglobulin heavy chain gene deletion at direct repeats: nucleotide sequence and effect on mRNA accumulation.

作者信息

Kobrin B, Glass K, Morrison S L, Milcarek C

机构信息

Department of Microbiology, Columbia University, New York, N.Y. 10032.

出版信息

Mol Immunol. 1988 Feb;25(2):181-7. doi: 10.1016/0161-5890(88)90066-1.

Abstract

The DNA from the mouse myeloma cell, I17, which produces aberrant gamma 2b heavy chain mRNAs, was cloned and sequenced. The I17 mutant, and its parent line 10.1, share a small deletion at the splice junction of the CH1 domain which results in the absence of CH1 sequences from the mRNA. In addition, the genomic DNA of I17 has a deletion of 253 nucleotides which fuses the CH2 and CH3 exons, causes a frameshift of the next 43 amino acids and results in a truncated protein. The deleted nucleotides are flanked by two direct repeats of the CAGCA pentamer in the normal gene. One copy of the repeat and the interposed DNA is removed in the mutant. The DNA deletion is colinear with the mRNA. Both I17 and 10.1 cells have decreased accumulation of the secretory-specific gamma 2b mRNA. The amounts of membrane-specific gamma 2b mRNA are also affected in the mutants.

摘要

从小鼠骨髓瘤细胞I17中提取了能产生异常γ2b重链mRNA的DNA,并进行了克隆和测序。I17突变体与其亲本细胞系10.1在CH1结构域的剪接连接处存在一个小缺失,导致mRNA中缺少CH1序列。此外,I17的基因组DNA有253个核苷酸的缺失,该缺失使CH2和CH3外显子融合,导致接下来的43个氨基酸发生移码,并产生截短的蛋白质。缺失的核苷酸在正常基因中两侧是CAGCA五聚体的两个直接重复序列。突变体中一个重复序列拷贝和插入的DNA被去除。DNA缺失与mRNA共线性。I17和10.1细胞中分泌特异性γ2b mRNA的积累均减少。突变体中膜特异性γ2b mRNA的量也受到影响。

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